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Mathilde Renaud

Showing results (11-20 of 79) with videos related to

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Parkinsonism & Related Disorders|October 18, 2019
Multiple System Atrophy: Phenotypic spectrum approach coupled with brain 18-FDG PETStephan Grimaldi, Mohamed Boucekine, Tatiana Witjas, et al.
Journal of Neurology|March 29, 2017
Subacute parkinsonism as a complication of Lyme diseaseGuillaume Pisché, Meriam Koob, Thomas Wirth, et al.
American Journal of Medical Genetics. Part A|May 25, 2026
Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith-Magenis SyndromeAlbin Blanc, Christophe Nemos, Céline Bonnet, et al.
Journal of Research on Adolescence : the Official Journal of the Society for Research on Adolescence|March 14, 2026
Longitudinal changes in sexual identity during adolescence and their associations with sexual well-beingAlice Girouard, Alexa Martin-Storey, Jacinthe Dion, et al.
Journal of Marital and Family Therapy|July 15, 2026
Cumulative Childhood Trauma and Relationship Distress: The Intermediary Role of Emotion Regulation Among Couples Seeking Relationship PsychotherapyMaria Belen Field Lira, Zoé Benoit, Laurie Raphaelle Beauvilliers, et al.
Parkinsonism & Related Disorders|February 21, 2023
Heterozygous pathogenic variation in GCH1 associated with treatable severe spastic tetraplegiaJean-Marie Ravel, Maud Michaud, Solène Frismand, et al.
BMC Neurology|November 25, 2016
A step toward essential tremor gene discovery: identification of extreme phenotype and screening of HTRA2 and ANO3Mathilde Renaud, Christophe Marcel, Gabrielle Rudolf, et al.
American Journal of Medical Genetics. Part A|August 16, 2022
First report of a short in-frame biallelic deletion removing part of the EGF-like domain calcium-binding motif in LTBP4 and causing autosomal recessive cutis laxa type 1CJean-Marie Ravel, Margot Comel, Marion Wandzel, et al.
Journal of Neurology|May 28, 2016
Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxiaMathilde Renaud, Claire Guissart, Martial Mallaret, et al.
Journal of Neurology|July 21, 2022
Next-generation sequencing: a decisive diagnostic aid for atypical Wilson's diseaseAmory Jardel, Céline Bonnet, Solène Frismand-Kryloff, et al.
Pageof 8

Showing results (11-20 of 79) with videos related to

Sort By:
Pageof 8
Parkinsonism & Related Disorders|October 18, 2019
Multiple System Atrophy: Phenotypic spectrum approach coupled with brain 18-FDG PETStephan Grimaldi, Mohamed Boucekine, Tatiana Witjas, et al.
Journal of Neurology|March 29, 2017
Subacute parkinsonism as a complication of Lyme diseaseGuillaume Pisché, Meriam Koob, Thomas Wirth, et al.
American Journal of Medical Genetics. Part A|May 25, 2026
Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith-Magenis SyndromeAlbin Blanc, Christophe Nemos, Céline Bonnet, et al.
Journal of Research on Adolescence : the Official Journal of the Society for Research on Adolescence|March 14, 2026
Longitudinal changes in sexual identity during adolescence and their associations with sexual well-beingAlice Girouard, Alexa Martin-Storey, Jacinthe Dion, et al.
Journal of Marital and Family Therapy|July 15, 2026
Cumulative Childhood Trauma and Relationship Distress: The Intermediary Role of Emotion Regulation Among Couples Seeking Relationship PsychotherapyMaria Belen Field Lira, Zoé Benoit, Laurie Raphaelle Beauvilliers, et al.
Parkinsonism & Related Disorders|February 21, 2023
Heterozygous pathogenic variation in GCH1 associated with treatable severe spastic tetraplegiaJean-Marie Ravel, Maud Michaud, Solène Frismand, et al.
BMC Neurology|November 25, 2016
A step toward essential tremor gene discovery: identification of extreme phenotype and screening of HTRA2 and ANO3Mathilde Renaud, Christophe Marcel, Gabrielle Rudolf, et al.
American Journal of Medical Genetics. Part A|August 16, 2022
First report of a short in-frame biallelic deletion removing part of the EGF-like domain calcium-binding motif in LTBP4 and causing autosomal recessive cutis laxa type 1CJean-Marie Ravel, Margot Comel, Marion Wandzel, et al.
Journal of Neurology|May 28, 2016
Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxiaMathilde Renaud, Claire Guissart, Martial Mallaret, et al.
Journal of Neurology|July 21, 2022
Next-generation sequencing: a decisive diagnostic aid for atypical Wilson's diseaseAmory Jardel, Céline Bonnet, Solène Frismand-Kryloff, et al.
Pageof 8